Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isonicotinic Acid | HCID 5922 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | p-Cyanobenzamide | HCID 76427 | — |
| Reactant | Pyridine-4-carbonyl chloride | HCID 417436 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 22058004 | HCID 22058004 | — |
Reaction Steps
A mixture of pyrid4-ylcarbonyl chloride (prepared by the reaction of pyridine-4-carboxylic acid and oxalyl chloride; 0.213 g), N-3-amino4-chlorophenyl)-4-cyanobenzamide (0.27 g) and pyridine (4 ml) was stirred and heated to 110° C. for 16 hours. After cooling, the mixture was poured into water (25 ml). The resultant precipitate was collected, washed with water and dried to give the title compound as a solid (0.32 g); NMR Spectrum: (DMSOd6) 7.58 (d, 1H), 7.75 (m, 1H), 7.85 (d, 2H), 8.01 (d, 2H), 8.10 (m, 3H), 8.80(d, 2H); Mass Spectrum: M+H+ 377.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06432949B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-8c673778f1c2425099ead8482afe1550 |
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| Source note | uspto-grants-2002_08 |
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